• 10995 Quivira Road, Overland Park, Kansas 66210, United States
  • Mon - Fri 8am - 5pm
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Current Studies

ONGOING CLINICAL TRIALS

Minimum Criteria

  • Male or female volunteers between 21 and 80 years of age at enrollment
  • Clinic at 1 month and 3-months follow-up and programming
  • Subjects receiving at least 50% reduction in their back pain, during the trial phase, will continue to the permanent implant phase

Minimum Criteria

  • Male or female volunteers older than 18 years of age 
  • Candidates for SCS system - back pain with or without leg pain 
  • Diagnosed with chronic, refractory axial low back pain 
  • Willing to give written informed consent 

Minimum Criteria

  • Male or female volunteers older than 45 years of age 
  • Persistent leg/buttock/groin pain, with or without back pain that is consistently relieved by flexion activities (ex. sitting or bending over)
  • Diagnosed with degenerative spinal stenosis
  • Willing to give written informed consent 

Minimum Criteria

  • Male or female volunteers between 30-70 years of age
  • Diagnosed with LDH with inadequate improvement in pain
  • Willing to give written informed consent

Minimum Criteria

  • Male or female volunteers 18 years of age or older 
  • History of persistent pain in the distribution of the sacroiliac joint despite adequate trail of physical therapy  
  • Willing to give written informed consent 

Minimum Criteria

  • Male or female volunteers 18 years of age or older 
  • Primary pain associated with PDPN in the feet   
  • Willing to give written informed consent 
  • Be able to comply with study regulations and visits 

Minimum Criteria

  • Male or female volunteers 18 years of age or older 
  • Documented diagnosis of PSNP   
  • Willing to give written informed consent 
  • Be able to comply with study regulations and visits 

Minimum Criteria

  • Male or female volunteers 18 years of age or older 
  • Documented diagnosis of cervical spondylosis and comorbidity of cervicogenic headache   
  • 6 month history of chronic, function-limiting neck pain and headache 
  • Willing to give written informed consent 
  • Be able to comply with study regulations and visits 

Minimum Criteria

  • Male or female volunteers 18 years of age or older 
  • Diagnosed with chronic, intractable pain of the back with or without leg pain  
  • Be on stable chronic pain medications, as determined by the PI 
  • Be able to comply with study regulations and visits 

Minimum Criteria

  • Male or female volunteers between the ages of 50-80
  • Pain in the leg/lower back with relief while bending forward or sitting down 
  • Be able to comply with study regulations and visits 

In order to patricipate in the following studies, individuals must be willing to give written informed consent. and be able to comply with study regulations and visits. Compensation may be provided for participation *

Study for individuals that have peripheral neuropathy as a result of chemotherapy

  • Onset of pain in hands or feet after prior treatment of cancer with taxanes or platins 
  • Painful symptoms can be accompanied by non painful symptoms (tingling/pins and needles, numbness)
  • Stopped chemotherapy treatment for at least 24 weeks 
  • Peripheral neuropathy pain for at least 24 weeks
  • Primary objective: Assess the efficacy and safety of a topical cream in cancer survivor adult patients with CIPN
  • 4 in person visits over the course of 13 weeks, $480.00 in compensation

Study for individuals that suffer from pain, numbness, and/or cramping in the legs

  • Diagnosed with moderate degenerative lumbar spinal stenosis
  • Peristent leg/buttock/ groin pain, with or without back pain that is consistenly relieved by flexion actives (such as sitting or bending over a shopping cart)
  • That are able to sit for 50 minutes without pain and to walk for 50 feet or more
  • That have NOT had surgery of the lumbar spine
  • 45 years or older
  • Primary objective: compile long-term outcomes of an implanted device in routine clinical practice 
  • 7 in person visits over the course of 5 years, $1,500.00 in compensation

Study for individuals that have significant pain due to diabetic peripheral neuropathy of the feet

  • Do not have any current foot ulcers, skin inflammation, infection, redness, swelling, or gangrene
  • Do not have hypersensitivity to capsaicin

Study for individuals that have chronic moderate to severe post surgical neuropathic pain

  • Has lasted for at least 6 months
 

Study for individuals that suffer from chronic, function-limiting neck pain and headache

  • Has lasted more than 6 months
  • Has not responded to other treatments (such as physical therapy, chiropractic care, bed rest, etc.)
 

Study for individuals with osteoarthritis of the knee

  • Diagnosed with osteoarthritis of the knee
  • Pain in index knee has been present for at least 6 months
  • Insufficient pain relief with standard of care:-
    1. Non-pharmacological treatment (physical therapy, exercise, muscle strengthening, etc.)
    2. 1 or more courses of oral non-steroidal anti inflammatory drugs
    3. where appropriate, opioids, steroid injections
  • Have NOT had joint replacement surgery of the index knee
  • Have NOT had a history of significant trauma or surgery to index knee in past year

Study for individuals with lumbar and/or lumbosacral radiculopathy

  • Pain must have radicular component that have been present for at least 8 weeks, but not longer than 9 months
  • Insufficient pain relief or improvement following at least 8 weeks of:
    1. Non-pharmacological/ mechanical treatment (physical therapy, exercise, chiropractic treatment, etc.)
    2. Over-the-counter analgesics (non-steroidal anti-inflammatories, topical gels, creams or ointments
  • Has NOT had lumbar surgery and/ or intradiscal interventions
  • Primary objective: study the efficacy and safety of a lumbar injection in the treatment of pain associated with lumbar radiculopathy
  • 7 in person and 6 phone visits over the course of 12 months, $1,530.00 in compensation
  • Onset of pain in hands or feet after prior treatment of cancer with taxanes or platins 
  • Painful symptoms can be accompanied by non painful symptoms (tingling/pins and needles, numbness)
  • Stopped chemotherapy treatment for at least 24 weeks 
  • Peripheral neuropathy pain for at least 24 weeks
  • Diagnosed with moderate degenerative lumbar spinal stenosis
  • Peristent leg/buttock/ groin pain, with or without back pain that is consistenly relieved by flexion actives (such as sitting or bending over a shopping cart)
  • That are able to sit for 50 minutes without pain and to walk for 50 feet or more
  • That have NOT had surgery of the lumbar spine
  • 45 years or older
  • Do not have any current foot ulcers, skin inflammation, infection, redness, swelling, or gangrene
  • Do not have hypersensitivity to capsaicin
  • Has lasted for at least 6 months
 
  • Has lasted more than 6 months
  • Has not responded to other treatments (such as physical therapy, chiropractic care, bed rest, etc.)
 
  • Without or without leg pain
  • Diagnosed with osteoarthritis of the knee
  • Pain in index knee has been present for at least 6 months
  • Insufficient pain relief with standard of care:-
    1. Non-pharmacological treatment (physical therapy, exercise, muscle strengthening, etc.)
    2. 1 or more courses of oral non-steroidal anti inflammatory drugs
    3. where appropriate, opioids, steroid injections
  • Have NOT had joint replacement surgery of the index knee
  • Have NOT had a history of significant trauma or surgery to index knee in past year
  • Pain must have radicular component that have been present for at least 8 weeks, but not longer than 9 months
  • Insufficient pain relief or improvement following at least 8 weeks of:
    1. non-pharmacological/ mechanical treatment (physical therapy, exercise, chiropractic treatment, etc.)
    2. over-the-counter analgesics (non-steroidal anti-inflammatories, topical gels, creams or ointments
  • Has NOT had lumbar surgery and/ or intradiscal interventions

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Contact us - (913)-825-2314

We love our patients, so feel free to ring during normal business hours and ask about current trials.

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Overland Park, Kansas - (Kansas City area)

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    10995 Quivira Road, Overland Park,
    Kansas 66210, United States

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